Thanks a ton for making this video and a great job at explaining the process thoroughly!
@amiraakilah89505 жыл бұрын
i ve been for 3 months in laboratory and i could not ever understand it until you explained it that was .. many many thanks , keep on
@prudencephodisomashile49093 жыл бұрын
This is awesome, thank you so much for such detailed explanation.
@JeanStorM3 жыл бұрын
Thanks so much! helpful and detailed video for beginner.
@dhruvkumarsoni53443 жыл бұрын
Very nicely explained. Thanks! Best wishes.
@palvoliuto60593 жыл бұрын
that was a fabulous video!!!!! clear, precise and detailed. thank you so much!!!!!!
@khalilelbadri5371 Жыл бұрын
Thank you for such amazing lecture.
@adronung18922 жыл бұрын
When you are talking about the olden days that is exactly what I do now. However, I syphon buffer onto the column so do I don't have to manually add buffer to the column, and I automatically collect fractions with a spin collector. I used Bradford assay to find the bluest fractions where the protein is present, and I check the A280 of those fractions.
@devikasharma24063 жыл бұрын
I loved this video....I have an interview at my workplace in Sydney please pray for me.
@shawnaguheen42703 жыл бұрын
Thanks so much!!
@LucasRegmi3 жыл бұрын
Great
@diponsaha53574 жыл бұрын
Thank you Dada
@syed-wd8ib3 жыл бұрын
How machine knows about the total volume used in elution?
@tamerwali4598 Жыл бұрын
Great, which you prefer this sys or NGC and why?
@SteSews2 жыл бұрын
Hello, I do have a probleme with my Akta system, the UV sensor doesn't work, I can't obtain a graph with UV variation. I do see the UV variation in the little screen wich is on the machine, but there is nothing on the graph so it's very hard to know where my samples are...Does anyone have an idea on how I can fix this please let me know ! thanks
@loveforbioinfo3 жыл бұрын
Nice video but too many repetitions which increases video time